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Lipid disorders
- Atypical cutaneous and musculoskeletal manifestation of SARS-CoV-2: ‘COVID-19 toes’ and spasticity in a 48-year-old womanAvery Kopacz, Cameron Ludwig, Michelle TarboxBMJ Case Reports CP Mar 2021, 14 (3) e241410; DOI: 10.1136/bcr-2020-241410
- Singular case of acanthosis nigricansCristiana Maximiano, Marta Ribeiro Silva, Maria Miguel Gomes, Ana AntunesBMJ Case Reports CP Feb 2021, 14 (2) e240143; DOI: 10.1136/bcr-2020-240143
- Flaxseed oil stimulates gynecomastiaTsuneo Takenaka, Mayuko Nagano, Koji Yamashita, Kiyoshi KikuchiBMJ Case Reports CP Dec 2020, 13 (12) e237948; DOI: 10.1136/bcr-2020-237948
- Extensive tendon and tuberous xanthomas in a patient with familial hypercholesterolaemiaAyan Roy, Sadishkumar Kamalanathan, Dukhabandhu Naik, Jaya Prakash SahooBMJ Case Reports CP Sep 2020, 13 (9) e236759; DOI: 10.1136/bcr-2020-236759
- Visible lipaemia in a man with early onset metabolic syndromeLuke Debenham, Jayashekara AcharyaBMJ Case Reports CP Aug 2020, 13 (8) e234824; DOI: 10.1136/bcr-2020-234824
- Milk-induced hypertriglyceridaemia and acute pancreatitis after discontinuation of treatment for type 2 diabetes and hyperlipidaemiaNeel Gautam Jain, Anya HargreavesBMJ Case Reports CP Aug 2019, 12 (8) e231562; DOI: 10.1136/bcr-2019-231562
- Update on management of hypertriglyceridaemia-induced acute pancreatitisKamal Kant Sahu, Ajay Kumar Mishra, Amos Lal, Eric S SilvermanBMJ Case Reports CP Aug 2019, 12 (8) e231703; DOI: 10.1136/bcr-2019-231703
- An enigmatic triad of acute pancreatitis, diabetic ketoacidosis and hypertriglyceridaemia: who is the culprit?Umasankar Mathuram Thiyagarajan, Amirthavarshini Ponnuswamy, Alex ChungBMJ Case Reports CP Jul 2019, 12 (7) e217272; DOI: 10.1136/bcr-2016-217272
- Familial hypertriglyceridaemia and type 2 diabetes in pregnancy: prevention of acute pancreatitis with diet control and omega-3 fatty acidsMelissa Ong, Lynne Jerreat, Aisha HameedBMJ Case Reports CP May 2019, 12 (5) e227321; DOI: 10.1136/bcr-2018-227321
- Severe hypertriglyceridaemia and pancreatitis in a patient with lipoprotein lipase deficiency based on mutations in lipoprotein lipase (LPL) and apolipoprotein A5 (APOA5) genesCharlotte Koopal, Remy Bemelmans, A David Marais, Frank LJ VisserenBMJ Case Reports CP Apr 2019, 12 (4) e228199; DOI: 10.1136/bcr-2018-228199
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